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J Koenig

Showing results (511-520 of 522) with videos related to

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Cancer Research|May 28, 2021
STK11/LKB1 Loss of Function Is Associated with Global DNA Hypomethylation and <i>S</i>-Adenosyl-Methionine Depletion in Human Lung AdenocarcinomaMichael J Koenig, Bernice A Agana, Jacob M Kaufman, et al.
Growth Hormone & IGF Research : Official Journal of the Growth Hormone Research Society and the International IGF Research Society|January 18, 2011
The severe short stature in two siblings with a heterozygous IGF1 mutation is not caused by a dominant negative effect of the putative truncated proteinH A van Duyvenvoorde, J van Doorn, J Koenig, et al.
Physical Review Letters|January 13, 2019
Logarithmic Upturn in Low-Temperature Electronic Transport as a Signature of d-Wave Order in Cuprate SuperconductorsXiaoqing Zhou, D C Peets, Benjamin Morgan, et al.
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology|March 23, 2006
Towards the molecular elucidation of congenital myasthenic syndromes: identification of mutations in MuSKF Chevessier, B Faraut, A Ravel-Chapuis, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|April 13, 2006
Delineation, functional validation, and bioinformatic evaluation of gene expression in thyroid follicular carcinomas with the PAX8-PPARG translocationThomas J Giordano, Amy Y M Au, Rork Kuick, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|August 22, 2019
Identification of Recurrent Activating <i>HER2</i> Mutations in Primary Canine Pulmonary AdenocarcinomaGwendolen Lorch, Karthigayini Sivaprakasam, Victoria Zismann, et al.
Neurology|December 10, 2008
The CHRNE 1293insG founder mutation is a frequent cause of congenital myasthenia in North AfricaP Richard, K Gaudon, H Haddad, et al.
Annals of Emergency Medicine|July 27, 2001
The model of the clinical practice of emergency medicineR S Hockberger, L S Binder, M A Graber, et al.
Journal of Neurology|December 17, 2009
Phenotype genotype analysis in 15 patients presenting a congenital myasthenic syndrome due to mutations in DOK7A Ben Ammar, F Petit, N Alexandri, et al.
JACC. Cardiovascular Interventions|May 26, 2009
Integration of pre-hospital electrocardiograms and ST-elevation myocardial infarction receiving center (SRC) networks: impact on Door-to-Balloon times across 10 independent regionsIvan C Rokos, William J French, William J Koenig, et al.
Pageof 53

Showing results (511-520 of 522) with videos related to

Sort By:
Pageof 53
Cancer Research|May 28, 2021
STK11/LKB1 Loss of Function Is Associated with Global DNA Hypomethylation and <i>S</i>-Adenosyl-Methionine Depletion in Human Lung AdenocarcinomaMichael J Koenig, Bernice A Agana, Jacob M Kaufman, et al.
Growth Hormone & IGF Research : Official Journal of the Growth Hormone Research Society and the International IGF Research Society|January 18, 2011
The severe short stature in two siblings with a heterozygous IGF1 mutation is not caused by a dominant negative effect of the putative truncated proteinH A van Duyvenvoorde, J van Doorn, J Koenig, et al.
Physical Review Letters|January 13, 2019
Logarithmic Upturn in Low-Temperature Electronic Transport as a Signature of d-Wave Order in Cuprate SuperconductorsXiaoqing Zhou, D C Peets, Benjamin Morgan, et al.
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology|March 23, 2006
Towards the molecular elucidation of congenital myasthenic syndromes: identification of mutations in MuSKF Chevessier, B Faraut, A Ravel-Chapuis, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|April 13, 2006
Delineation, functional validation, and bioinformatic evaluation of gene expression in thyroid follicular carcinomas with the PAX8-PPARG translocationThomas J Giordano, Amy Y M Au, Rork Kuick, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|August 22, 2019
Identification of Recurrent Activating <i>HER2</i> Mutations in Primary Canine Pulmonary AdenocarcinomaGwendolen Lorch, Karthigayini Sivaprakasam, Victoria Zismann, et al.
Neurology|December 10, 2008
The CHRNE 1293insG founder mutation is a frequent cause of congenital myasthenia in North AfricaP Richard, K Gaudon, H Haddad, et al.
Annals of Emergency Medicine|July 27, 2001
The model of the clinical practice of emergency medicineR S Hockberger, L S Binder, M A Graber, et al.
Journal of Neurology|December 17, 2009
Phenotype genotype analysis in 15 patients presenting a congenital myasthenic syndrome due to mutations in DOK7A Ben Ammar, F Petit, N Alexandri, et al.
JACC. Cardiovascular Interventions|May 26, 2009
Integration of pre-hospital electrocardiograms and ST-elevation myocardial infarction receiving center (SRC) networks: impact on Door-to-Balloon times across 10 independent regionsIvan C Rokos, William J French, William J Koenig, et al.
Pageof 53